Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA

被引:4
作者
Kazemi, Tina [1 ]
Avci, Naze G. [1 ]
Keller, Renee F. [1 ]
Akay, Yasemin M. [1 ]
Akay, Metin [1 ]
机构
[1] Univ Houston, Dept Biomed Engn, Houston, TX 77204 USA
关键词
VENTRAL TEGMENTAL AREA; DOPAMINE NEURONS; GLUTAMATE NEURONS; TYROSINE-HYDROXYLASE; SUBSTANTIA-NIGRA; MIDBRAIN; BRAIN; PREGNANCY; TRANSPORTER; EXPRESSION;
D O I
10.1038/s41598-020-59248-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chronic nicotine exposure during pregnancy has been shown to induce physiological and anatomical alterations in offspring. Previously, we investigated the complexity of dopamine (DA) neuron firing in the sub-regions of the ventral tegmental area (VTA) following perinatal nicotine exposure. Using approximate entropy, we found that within the middle sub-region, the parainterfascicular nucleus (PIF), there was higher complexity indicating more random neural firing and a less homogeneous neuron population. Therefore, we sought to investigate the neuron populations within the sub-regions of the VTA following perinatal nicotine exposure. We used real time PCR in order to find the relative quantity of glutamate to gamma-aminobutyric acid (GABA), DA, and glutamate neurons within three sub-regions: the parabrachial pigmented nucleus (PBP), parainterfascicular nucleus (PIF), and paranigral nucleus (PN). Our results showed that the PIF region of the VTA contained a more diverse population of neurons resulting in a more complex system. In addition, we found that DA neurons are more activated in PN sub-region of the VTA, which mediates the rewarding effects of drugs including nicotine. Lastly, using immunohistochemistry, we observed an overall decrease in DA neurons following perinatal nicotine exposure.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] [Anonymous], 2006, The Health Consequences of Involuntary Exposure to Tobacco Smoke: A Report of the Surgeon General
  • [2] CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING
    BENJAMINI, Y
    HOCHBERG, Y
    [J]. JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) : 289 - 300
  • [3] VGLUT2 in dopamine neurons is required for psychostimulant-induced behavioral activation
    Birgner, Carolina
    Nordenankar, Karin
    Lundblad, Martin
    Mendez, Jose Alfredo
    Smith, Casey
    le Greves, Madeleine
    Galter, Dagmar
    Olson, Lars
    Fredriksson, Anders
    Trudeau, Louis-Eric
    Kullander, Klas
    Wallen-Mackenzie, Asa
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (01) : 389 - 394
  • [4] Dopamine neuron systems in the brain:: an update
    Bjorklund, Anders
    Dunnett, Stephen B.
    [J]. TRENDS IN NEUROSCIENCES, 2007, 30 (05) : 194 - 202
  • [5] Center for Health Promotion and Education. Office on Smoking and Health. United States Publich Health Services. Office of the Surgeon General, 1988, HLTH CONS SMOK NIC A
  • [6] Centers for Disease Control and Prevention (CDC), 2002, MMWR Morb Mortal Wkly Rep, V51, P300
  • [7] Gestational nicotine exposure reduces nicotinic cholinergic receptor (nAChR) expression in dopaminergic brain regions of adolescent rats
    Chen, H
    Parker, SL
    Matta, SG
    Sharp, BM
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2005, 22 (02) : 380 - 388
  • [8] The effects of nicotine exposure and PFC transection on the time-frequency distribution of VTA DA neurons' firing activities
    Chen, Ting Y.
    Zhang, Die
    Dragomir, Andrei
    Akay, Yasemin
    Akay, Metin
    [J]. MEDICAL & BIOLOGICAL ENGINEERING & COMPUTING, 2011, 49 (05) : 605 - 612
  • [9] Developmental consequences of prenatal tobacco exposure
    Cornelius, Marie D.
    Day, Nancy L.
    [J]. CURRENT OPINION IN NEUROLOGY, 2009, 22 (02) : 121 - 125
  • [10] Neuronal Nicotinic Acetylcholine Receptor Structure and Function and Response to Nicotine
    Dani, John A.
    [J]. NICOTINE USE IN MENTAL ILLNESS AND NEUROLOGICAL DISORDERS, 2015, 124 : 3 - 19